Arjan Bouman

630 total citations
14 papers, 146 citations indexed

About

Arjan Bouman is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Arjan Bouman has authored 14 papers receiving a total of 146 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Arjan Bouman's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Congenital heart defects research (3 papers). Arjan Bouman is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Congenital heart defects research (3 papers). Arjan Bouman collaborates with scholars based in Netherlands, United States and Germany. Arjan Bouman's co-authors include Anne-Marie Van Der Kevie-Kersemaekers, Rolph Pfundt, Tjitske Kleefstra, Stefan Gröschel, Marcel M. A. M. Mannens, Erwin Brosens, Barış Karakullukçu, Edward Blair, Ruud Delwel and Willem H. Schreuder and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.

In The Last Decade

Arjan Bouman

14 papers receiving 133 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Arjan Bouman Netherlands	8	73	68	21	21	21	14	146
Constance Wells France	7	61 0.8×	49 0.7×	23 1.1×	10 0.5×	6 0.3×	11	124
Stacey Hume Canada	10	68 0.9×	108 1.6×	30 1.4×	16 0.8×	3 0.1×	19	207
Vyne van der Schoot Netherlands	8	98 1.3×	48 0.7×	56 2.7×	16 0.8×	20 1.0×	15	182
Peter Walter Germany	5	80 1.1×	131 1.9×	9 0.4×	19 0.9×	15 0.7×	16	230
Aman Kumar India	8	26 0.4×	140 2.1×	11 0.5×	21 1.0×	18 0.9×	19	295
Neda Zadeh United States	7	141 1.9×	152 2.2×	28 1.3×	6 0.3×	4 0.2×	12	253
Milena Simioni Brazil	9	195 2.7×	125 1.8×	33 1.6×	23 1.1×	11 0.5×	26	272
Soyoung Jeon South Korea	8	23 0.3×	95 1.4×	19 0.9×	7 0.3×	6 0.3×	23	169
Maryam Rafati Iran	6	17 0.2×	45 0.7×	16 0.8×	3 0.1×	14 0.7×	22	90
Richard Lao United States	4	68 0.9×	51 0.8×	4 0.2×	3 0.1×	9 0.4×	7	117

Countries citing papers authored by Arjan Bouman

Since Specialization

Citations

This map shows the geographic impact of Arjan Bouman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Arjan Bouman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arjan Bouman more than expected).

Fields of papers citing papers by Arjan Bouman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arjan Bouman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Arjan Bouman. The network helps show where Arjan Bouman may publish in the future.

Co-authorship network of co-authors of Arjan Bouman

This figure shows the co-authorship network connecting the top 25 collaborators of Arjan Bouman. A scholar is included among the top collaborators of Arjan Bouman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Arjan Bouman. Arjan Bouman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Jia, Xiangbin, Mariëlle Alders, Arjan Bouman, et al.. (2022). De novo variants in the PABP domain of PABPC1 lead to developmental delay. Genetics in Medicine. 24(8). 1761–1773. 4 indexed citations

Haarman, Annechien E. G., Alberta A. H. J. Thiadens, Marianne van Tienhoven, et al.. (2022). Whole exome sequencing of known eye genes reveals genetic causes for high myopia. Human Molecular Genetics. 31(19). 3290–3298. 23 indexed citations

Verhoeven, Virginie J. M., Annechien E. G. Haarman, Jan Roelof Polling, et al.. (2020). Diagnostic exome sequencing in 50 patients with high myopia. Investigative Ophthalmology & Visual Science. 61(7). 2673–2673. 1 indexed citations

Henneman, Peter, Arjan Bouman, Adri N. Mul, et al.. (2018). Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates. PLoS ONE. 13(3). e0194938–e0194938. 20 indexed citations

Bouman, Arjan, Quinten Waisfisz, Rick R. van Rijn, et al.. (2018). Homozygous DMRT2 variant associates with severe rib malformations in a newborn. American Journal of Medical Genetics Part A. 176(5). 1216–1221. 10 indexed citations

Bouman, Arjan, Mieke M. van Haelst, & Rosalina van Spaendonk. (2018). Blepharophimosis–ptosis–epicanthus inversus syndrome caused by a 54-kb microdeletion in a FOXL2 cis-regulatory element. Clinical Dysmorphology. 27(2). 58–62. 4 indexed citations

Bouman, Arjan, Alice S. Brooks, & Marjon A. van Slegtenhorst. (2018). [Whole Exome Sequencing in daily practice: the possibilities and impossibilities of this diagnostic test].. PubMed. 162. 2 indexed citations

Bouman, Arjan, Silvana van Koningsbruggen, Barış Karakullukçu, Willem H. Schreuder, & Phillis Lakeman. (2017). Bloom syndrome does not always present with sun-sensitive facial erythema. European Journal of Medical Genetics. 61(2). 94–97. 12 indexed citations

Bouman, Arjan, et al.. (2017). Oral‐facial‐digital syndrome type 1 in males: Congenital heart defects are included in its phenotypic spectrum. American Journal of Medical Genetics Part A. 173(5). 1383–1389. 10 indexed citations

10.

Bouman, Arjan, et al.. (2016). Trisomy 4 mosaicism: Delineation of the phenotype. American Journal of Medical Genetics Part A. 170(4). 1040–1045. 2 indexed citations

11.

Bouman, Arjan, Stefan Gröschel, Claudia Erpelinck-Verschueren, et al.. (2015). Congenital thrombocytopenia in a neonate with an interstitial microdeletion of 3q26.2q26.31. American Journal of Medical Genetics Part A. 170(2). 504–509. 13 indexed citations

12.

Bouman, Arjan, Marjan M. Weiss, Sandra Jansen, et al.. (2015). An interstitial de-novo microdeletion of 3q26.33q27.3 causing severe intrauterine growth retardation. Clinical Dysmorphology. 24(2). 68–74. 7 indexed citations

13.

Neuhann, Teresa, Angelika Rieß, Edward Blair, et al.. (2015). ADAMTSL4‐associated isolated ectopia lentis: Further patients, novel mutations and a detailed phenotype description. American Journal of Medical Genetics Part A. 167(10). 2376–2381. 18 indexed citations

14.

Bouman, Arjan, et al.. (2013). Clinical delineation of a patient with trisomy 12q23q24. European Journal of Medical Genetics. 56(8). 463–469. 20 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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